Canonical Allele Identifier: PA658665988
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467289
ClinVar RCV Id: RCV000555385 RCV000597681 RCV000727403 RCV003150266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg18784His
CA1993265
NM_001267550.2:c.56351G>A